EMA, Guideline on the quality of water for pharmaceutical use, 07/20 Anna Sandberg2023-06-09T07:20:50+00:00September 28th, 2021|
FDA Inspection Technical Guide No 36, Reverse Osmosis, 10/80 2021-09-22T14:10:27+00:00January 17th, 2020|
EMA Guideline on the sterilisation of medicinal product, active substance, excipient and primary container, 03/19 Lars-Eric Ellow2023-06-09T07:21:08+00:00December 10th, 2019|
EU GMP Guide. Annex 01, Manufacture of sterile medicinal products, 03/20 DRAFT 2020-07-29T13:19:43+00:00November 20th, 2019|
EMA Q&A on production of water for injections by non-distillation methods – RO and biofilms and control strategies, 06/16 DRAFT 2021-09-17T13:35:43+00:00November 20th, 2019|
FDA MAPP 5040.1 Product Quality Microbiology Information in the Common Technical Document – Quality (CTD-Q), 01/17 2021-09-22T14:12:00+00:00November 20th, 2019|